Atypical hemolytic uremic syndrome multigene analysis:Find:Pt:Bld/Tiss:Doc:Molgen

Preferred Label : Atypical hemolytic uremic syndrome multigene analysis:Find:Pt:Bld/Tiss:Doc:Molgen;

LOINC status : ACTIVE;

LOINC display name : Atypical hemolytic uremic syndrome multigene analysis Molgen Doc (Bld/Tiss);

LOINC long common name : Atypical hemolytic uremic syndrome multigene analysis in Blood or Tissue by Molecular genetics method;

LOINC short name : aHUS multigene analysis Bld/T;

LOINC description : Multigene testing for atypical hemolytic uremic syndrome (aHUS), a condition that can begin in the neonatal period to adulthood and consists of hemolytic anemia, thrombocytopenia, and renal failure caused by platelet thrombi in the kidney and other organs. Genes associated with genetic aHUS include C3, C5, CD46, CFB, CFH, CFHR1, CFHR2, CFHR3, CFHR4, CFHR5, CFI, DGKE, PLG, THBD, and MMACHC. Testing is performed for diagnostic, prognostic, and therapeutic assessment in patients with aHUS.[NCBI Books: NBK1367];

Details

Origin ID

99967-2;

UMLS CUI

C5570487;

Has component
- Atypical hemolytic uremic syndrome multigene analysis [LOINC component]
Has method
- Molecular genetics [LOINC method]
Has property
- Finding [LOINC Property]
Has scale
- Doc [LOINC scale]
Has system
- Blood [LOINC System]
- Blood or Tissue [LOINC System]
- Tissue and Smears [LOINC System]
Has time aspect
- Point in time (spot) [LOINC time aspect]
Semantic type(s)
- Clinical Attribute [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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